中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Potent anti-hepatoma efficacy of HCCS1 via dual tumor-targeting gene-virotherapy strategy

文献类型:期刊论文

作者Zhang, J; Gan, Y; Gu, JF; Hu, JY; Liu, XY; Zhao, XT
刊名ONCOLOGY REPORTS
出版日期2008
卷号20期号:5页码:1035-1040
关键词hepatocellular carcinoma suppressor 1 conditionally replication-competent adenovirus progression elevated gene-3 promoter gene therapy hepatocellular carcinoma
通讯作者Zhao, XT (reprint author), Shanghai Canc Inst, Cellular & Mol Immunol Lab, Shanghai 200032, Peoples R China.,xtzhao@online.sh.cn
英文摘要We previously demonstrated that hepatocellular carcinoma suppressor 1 (HCCS1) exerts potent anti-tumor activity. In this study, we constructed a new dual tumor-targeting oncolytic adenovirus vector, PD55-HCCS1, in which E1A was driven by the promoter of progression elevated gene-3, which is hepatoma-specific, and a CMV-HCCS1 expression cassette replaced E1B55. The PD55-HCCS1-mediated selective expression of E1A and HCCS1 in hepatoma cells and tumor-selective cytotoxicity in vitro and in vivo demonstrated the strongest inhibition of BEL-7404 cell xenografts in nude mice among a number of control Ad vectors. These data indicated the efficacy and safety of the PD55-HCCS1 system for HCC treatment.
学科主题Oncology
类目[WOS]Oncology
关键词[WOS]HUMAN HEPATOCELLULAR-CARCINOMA ; CHROMOSOME 17P13.3 ; THERAPY ; ADENOVIRUS ; CANCER ; REPLICATION ; CELLS ; PROGRESSION ; EXPRESSION ; PROMOTER
收录类别SCI
语种英语
WOS记录号WOS:000260648200006
版本出版稿
源URL[http://202.127.25.143/handle/331003/1371]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
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GB/T 7714
Zhang, J,Gan, Y,Gu, JF,et al. Potent anti-hepatoma efficacy of HCCS1 via dual tumor-targeting gene-virotherapy strategy[J]. ONCOLOGY REPORTS,2008,20(5):1035-1040.
APA Zhang, J,Gan, Y,Gu, JF,Hu, JY,Liu, XY,&Zhao, XT.(2008).Potent anti-hepatoma efficacy of HCCS1 via dual tumor-targeting gene-virotherapy strategy.ONCOLOGY REPORTS,20(5),1035-1040.
MLA Zhang, J,et al."Potent anti-hepatoma efficacy of HCCS1 via dual tumor-targeting gene-virotherapy strategy".ONCOLOGY REPORTS 20.5(2008):1035-1040.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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